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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02796183
Other study ID # 2015-1
Secondary ID
Status Completed
Phase N/A
First received June 7, 2016
Last updated June 9, 2016
Start date January 2015
Est. completion date May 2016

Study information

Verified date June 2016
Source Neon Hospital
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Interventional

Clinical Trial Summary

This study evaluates the effects of subconjunctivally injected bevacizumab in patients with diffuse diabetic macular edema.


Description:

At baseline, the macular thicknesses of both eyes of the patients with persistant diabetic macular edema were measured by optical coherence tomography. After 3.75mg bevacizumab was injected into subconjunctival space of the eyes with diabetic macular edema. The measurements of the macular thicknesses were repeated by optical coherence tomography in 15th, 30th, 60th day after injections. The macular thickness measurements before and after injection were compared.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date May 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Having diffuse diabetic macular edema persisted at least 1 month

- No intravitreal injection in last 3 months.

- No retinal laser photocoagulation in last 6 months

- Not have any other macular disease causing macular edema

Exclusion Criteria:

- Having ischemic macula

- Intravitreal injection in last 3 months.

- Retinal laser photocoagulation in last 6 months

- Have any other macular disease causing macular edema

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Subconjunctival bevacizumab (Altuzan)
Subconjunctival injections of Altuzan 3.75mg were applied in order to eliminate the macular edema.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Neon Hospital Ondokuz Mayis University

Outcome

Type Measure Description Time frame Safety issue
Primary Central Macular Thickness one year (between May 2015 and May 2016) No
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